Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP131653.RAi7zj0p7PwLrch2xPVNhL75z8PphpJ7eGCXlJ-catraM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP131653.RAi7zj0p7PwLrch2xPVNhL75z8PphpJ7eGCXlJ-catraM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP131653.RAi7zj0p7PwLrch2xPVNhL75z8PphpJ7eGCXlJ-catraM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP131653.RAi7zj0p7PwLrch2xPVNhL75z8PphpJ7eGCXlJ-catraM130_provenance.
- NP131653.RAi7zj0p7PwLrch2xPVNhL75z8PphpJ7eGCXlJ-catraM130_assertion description "[A significant increase in allele frequencies of 128R of E-selectin and the associated genotype SR was observed in celiac disease patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP131653.RAi7zj0p7PwLrch2xPVNhL75z8PphpJ7eGCXlJ-catraM130_provenance.
- NP131653.RAi7zj0p7PwLrch2xPVNhL75z8PphpJ7eGCXlJ-catraM130_assertion evidence source_evidence_literature NP131653.RAi7zj0p7PwLrch2xPVNhL75z8PphpJ7eGCXlJ-catraM130_provenance.
- NP131653.RAi7zj0p7PwLrch2xPVNhL75z8PphpJ7eGCXlJ-catraM130_assertion SIO_000772 16916660 NP131653.RAi7zj0p7PwLrch2xPVNhL75z8PphpJ7eGCXlJ-catraM130_provenance.
- NP131653.RAi7zj0p7PwLrch2xPVNhL75z8PphpJ7eGCXlJ-catraM130_assertion wasDerivedFrom lhgdn-20090331 NP131653.RAi7zj0p7PwLrch2xPVNhL75z8PphpJ7eGCXlJ-catraM130_provenance.
- NP131653.RAi7zj0p7PwLrch2xPVNhL75z8PphpJ7eGCXlJ-catraM130_assertion wasGeneratedBy ECO_0000203 NP131653.RAi7zj0p7PwLrch2xPVNhL75z8PphpJ7eGCXlJ-catraM130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP131653.RAi7zj0p7PwLrch2xPVNhL75z8PphpJ7eGCXlJ-catraM130_provenance.